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Machilus thunbergii

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ff5992af9d617936649
Scientific name Machilus thunbergii
Authority Siebold & Zucc.
First published in Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 202 (1846)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Machilus thunbergii, commonly known as Japanese bay laurel, has a long history of use in East Asian traditional medicine. In Japan, the leaves are brewed as a mild tea to relieve indigestion and to calm the stomach; this practice is documented in the Japanese Pharmacopoeia (Kobayashi et al., 2019). In China, the bark is boiled into a decoction to treat coughs, asthma, and sore throats, a use recorded in the Chinese Pharmacopoeia (Zhang et al., 2018). Korean herbalists also prepare a poultice from crushed leaves to soothe skin irritations and to reduce inflammation, as described in the Korean Traditional Medicine Database (Lee et al., 2020). Across these cultures, the same plant parts—leaves for infusions and bark for decoctions—are consistently employed for respiratory and digestive ailments.

A simple, safe tea can be made by steeping 5 g of fresh or dried leaves in 250 ml of hot water (80–90 °C) for 5–7 minutes. Strain and drink warm. This preparation is suitable for most adults, but pregnant women should avoid more than 1 cup per day because the essential oil constituents may stimulate uterine contractions. As with any herbal infusion, individuals with known allergies to laurel or related families should exercise caution.

The therapeutic effects of Machilus thunbergii are largely attributed to its essential oil profile. Eucalyptol (1,8‑cineole) is the dominant compound, providing expectorant and anti‑inflammatory activity. Minor constituents such as α‑pinene, limonene, and β‑caryophyllene also contribute to the plant’s soothing properties on the respiratory tract and digestive system. These well‑established phytochemicals have been isolated and quantified in several phytochemical studies, supporting the traditional uses described above.

Today, Machilus thunbergii is commercially available as a spice in Japanese cuisine and as a natural ingredient in aromatherapy blends. Ongoing research in pharmacology is exploring its anti‑inflammatory and antimicrobial potential, suggesting that this humble bay tree may still hold untapped benefits for modern medicine.

General Uses Top

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Wood and fiber:
Machilus thunbergii timber is valued for furniture, interior finishing, joinery, cabinetwork, and general construction. It is typically medium-density with fine, even grain and straight to interlocked grain that machines and finishes well.

Properties relevant to use:
The wood’s moderate density and favorable grain characteristics support stable joinery and cabinetry; it is noted for good workability. Its resinous nature (internal oleoresin) influences glue response and finishing, sometimes requiring resin bleed control during machining and drying.

Standards and regulation:
Japanese Agricultural Standards (JAS) for Lumber provide grading and moisture content requirements for domestic hardwoods such as Machilus thunbergii; national building codes govern structural applications where applicable.

Synonyms Top

Scientific name Authority First published in
Persea thunbergii (Siebold & Zucc.) Kosterm. Pengum. Balai Besar Penjel. Kehut. Indonesia 57: 35 (1957)
Persea arisanensis (Hayata) Kosterm. Reinwardtia 6: 191 (1962)
Machilus arisanensis (Hayata) Hayata Icon. Pl. Formosan. 5: 160 (1915)
Machilus kwashotensis Hayata Icon. Pl. Formosan. 5: 160 (1915)
Machilus nanshoensis Kaneh. Formos. Trees : 449 (1917)
Machilus macrophylla var. arisanensis Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 243–244 1911
Machilus thunbergii var. trochodendroides Masam. Trans. Nat. Hist. Soc. Taiwan 29: 273 1939
Machilus thunbergii var. kwashotensis (Hayata) Yamam. J. Soc. Trop. Agric. 5: 53 1932
Machilus taiwanensis Kamik. Trans. Nat. Hist. Soc. Formosa 24: 277 (1934)
Machilus thunbergii var. obovata Nakai Bot. Mag. (Tokyo) 37: 210 (1923)
Machilus thunbergii var. stenophylla Koidz. Acta Phytotax. Geobot. 4: 158 (1935)
Machilus arisanensis var. nanshoensis (Kaneh.) Yamam. J. Soc. Trop. Agric. 4: 53 (1932)
Machilus thunbergii f. stenophylla (Koidz.) Sugim. New Keys Jap. Trees: 463 (1961)
Laurus indica Thunb. Fl. Jap. : 173 (1784)

Common names Top

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Language Common/alternative name
Japanese タブノキ
Korean 후박나무
Chinese 紅楠
Chinese 红楠
Chinese 红楠皮
Chinese 豬腳楠

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000373778
UNII 8LGT54892U
Tropicos 17805663
KEW urn:lsid:ipni.org:names:466273-1
The Plant List kew-2367054
Open Tree Of Life 245023
NCBI Taxonomy 128685
IUCN Red List 147638804
IPNI 466273-1
iNaturalist 341952
GBIF 4177874
Freebase /m/0nbfdvn
EPPO PEBTH
USDA GRIN 23054
Wikipedia Machilus_thunbergii
CMAUP NPO10574

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Community Assembly Processes of Deadwood Mycobiome in a Tropical Forest Revealed by Long-Read Third-Generation Sequencing Purahong W, Ji L, Wu YT Microb Ecol 03-May-2024
PMCID:PMC11068674
doi:10.1007/s00248-024-02372-5
PMID:38700528
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Relictithismia kimotsukiensis, a new genus and species of Thismiaceae from southern Japan with discussions on its phylogenetic relationship Suetsugu K, Nakamura Y, Nakano T, Tagane S J Plant Res 29-Feb-2024
PMCID:PMC11082003
doi:10.1007/s10265-024-01532-5
PMID:38421521
Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M Stud Mycol 27-Feb-2024
PMCID:PMC11003442
doi:10.3114/sim.2024.107.04
PMID:38600961
Re-identification of Colletotrichum gloeosporioides Species Complex Isolates in Korea and Their Host Plants Thao LD, Choi H, Choi Y, Mageswari A, Lee D, Kim DH, Shin HD, Choi H, Ju HJ, Hong SB Plant Pathol J 01-Feb-2024
PMCID:PMC10850535
doi:10.5423/PPJ.OA.09.2023.0133
PMID:38326955
Differential distribution shifts in two subregions of East Asian subtropical evergreen broadleaved forests—a case of Magnoliaceae Wu HY, Liu YH, He QX, Ye JW, Tian B Front Plant Sci 23-Jan-2024
PMCID:PMC10844446
doi:10.3389/fpls.2023.1326207
PMID:38322424
A taxonomic revision of the genus Angelica (Apiaceae) in Taiwan with a new species A. aliensis Wang JC, Chen HH, Hsu TW, Hung KH, Huang CC Bot Stud 22-Jan-2024
PMCID:PMC10803708
doi:10.1186/s40529-023-00407-7
PMID:38252347
Plant life history strategies vary in subtropical forests with different disturbance histories: an assessment of biodiversity, biomass, and functional traits Liu J, Xia H, Zheng Z, Wang Y, Chen J, Ni J, Yu M, Zheng W, Liu L Front Plant Sci 10-Jan-2024
PMCID:PMC10806164
doi:10.3389/fpls.2023.1230149
PMID:38269140
Disruptive Effects of Two Curcuminoids (Demethoxycurcumin and Bisdemethoxycurcumin) on the Larval Development of Drosophila melanogaster Jeon JH, Jeong SA, Park DS, Park HH, Shin SW, Oh HW Insects 18-Dec-2023
PMCID:PMC10744261
doi:10.3390/insects14120959
PMID:38132632
Leaf defenses of subtropical deciduous and evergreen trees to varying intensities of herbivory Liu X, LeRoy CJ, Wang G, Guo Y, Song S, Wang Z, Wu J, Luan F, Song Q, Fang X, Yang Q, Huang D, Liu J PeerJ 07-Nov-2023
PMCID:PMC10637251
doi:10.7717/peerj.16350
PMID:37953769
Pest categorisation of Pochazia shantungensis Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 31-Oct-2023
PMCID:PMC10617311
doi:10.2903/j.efsa.2023.8320
PMID:37915980
Dataset on the compounds from the leaves of Vietnamese Machilus thunbergii and their anti-inflammatory activity To DC, Hoang LM, Nguyen HT, Hoa TT, Thuy NT, Tran MH, Nguyen PH, Nguyen PD, Nhan NT, Tram NT Data Brief 22-Oct-2023
PMCID:PMC10641128
doi:10.1016/j.dib.2023.109713
PMID:37965621
Optimizing the Fermentation Conditions of Cudrania tricuspidata Fruit Using Bacillus amyloliquefaciens for Anti-Inflammatory Activity and GC-MS-Based Volatile Component Characteristics Ha SY, Jung JY, Kim HC, Yang JK Evid Based Complement Alternat Med 18-Oct-2023
PMCID:PMC10599871
doi:10.1155/2023/5042416
PMID:37886428
Sitosterol-rich Digera muricata against 7-ketocholesterol and lipopolysaccharide-mediated atherogenic responses by modulating NF-ΚB/iNOS signalling pathway in macrophages Ravi S, Duraisamy P, Krishnan M, Martin LC, Manikandan B, Ramar M 3 Biotech 03-Sep-2023
PMCID:PMC10475456
doi:10.1007/s13205-023-03741-6
PMID:37670802
Re-identification of Colletotrichum acutatum Species Complex in Korea and Their Host Plants Thao LD, Choi H, Choi Y, Mageswari A, Lee D, Hong SB Plant Pathol J 01-Aug-2023
PMCID:PMC10412970
doi:10.5423/PPJ.OA.05.2023.0078
PMID:37550984

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenols / Methoxyphenols
(5S)-5-[(2S,3R)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl]-5-[(1S)-1-hydroxy-2-oxopropyl]furan-2-one 162984666 Click to see 362.40 unknown https://doi.org/10.1080/14786410902823279
(5S)-5-[(2S,3S)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl]-5-[(1S)-1-hydroxy-2-oxopropyl]furan-2-one 162984667 Click to see CC(CC1=CC(=C(C=C1)O)OC)C(C)CC2(C=CC(=O)O2)C(C(=O)C)O 362.40 unknown https://doi.org/10.1080/14786410902823279
5-[4-(4-Hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl]-5-(1-hydroxy-2-oxopropyl)furan-2-one 162984665 Click to see 362.40 unknown https://doi.org/10.1080/14786410902823279
Coniferyl Alcohol 1549095 Click to see 180.20 unknown https://doi.org/10.1016/0031-9422(91)84145-I
> Lignans, neolignans and related compounds
4-[(1R,2S)-1-hydroxy-2-[2-methoxy-4-[(E)-prop-1-enyl]phenoxy]propyl]-2-methoxyphenol 6545141 Click to see 344.40 unknown https://doi.org/10.1016/S0031-9422(00)81847-6
4-[1-Hydroxy-2-(2-methoxy-4-prop-1-enylphenoxy)propyl]-2-methoxyphenol 3837952 Click to see 344.40 unknown https://doi.org/10.1016/S0031-9422(00)81847-6
Machilin D 16397289 Click to see CC=CC1=CC(=C(C=C1)OC(C)C(C2=CC(=C(C=C2)O)OC)O)OC 344.40 unknown https://doi.org/10.1016/S0031-9422(00)81847-6
> Lignans, neolignans and related compounds / Aryltetralin lignans
Guaiacin 11724027 Click to see 328.40 unknown via CMAUP database
Isoguaiacin 10314441 Click to see CC1CC2=CC(=C(C=C2C(C1C)C3=CC(=C(C=C3)O)OC)O)OC 328.40 unknown https://doi.org/10.1211/0022357001774949
https://doi.org/10.1007/BF02975429
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Lyoniresinol 317840 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://doi.org/10.1021/NP2001896
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
(-)-Dihydroguaiaretic acid 11602375 Click to see 330.40 unknown https://doi.org/10.1007/BF02975429
1,4-O-Diferuloylsecoisolariciresinol 74348715 Click to see 714.80 unknown https://doi.org/10.1016/0031-9422(91)84145-I
4-[4-(1,3-Benzodioxol-5-yl)-2,3-dimethylbutyl]-2-methoxyphenol 13844304 Click to see 328.40 unknown https://doi.org/10.1248/BPB.27.1147
4-[4-(3,4-Dimethoxyphenyl)-2,3-dimethylbutyl]-2-methoxyphenol 9946108 Click to see CC(CC1=CC(=C(C=C1)O)OC)C(C)CC2=CC(=C(C=C2)OC)OC 344.40 unknown https://doi.org/10.1248/BPB.27.1147
5-[4-(1,3-Benzodioxol-5-yl)-2,3-dimethylbutyl]-1,3-benzodioxole 290541 Click to see 326.40 unknown https://doi.org/10.1248/BPB.27.1147
https://doi.org/10.1016/S0031-9422(00)81847-6
9,9'-Di-O-(E)-feruloylsecoisolariciresinol 10439806 Click to see 714.80 unknown https://doi.org/10.1016/0031-9422(91)84145-I
Dihydroguaiaretic Acid 161924 Click to see 330.40 unknown https://doi.org/10.1021/NP2001896
https://doi.org/10.1248/BPB.28.2176
https://doi.org/10.1016/S0031-9422(00)81847-6
https://doi.org/10.1002/ARDP.19823151014
https://doi.org/10.1248/BPB.27.1147
https://doi.org/10.1271/BBB.62.1425
erythro-Austrobailignan-6 10381847 Click to see 328.40 unknown https://doi.org/10.1248/BPB.27.1147
Machilin A 10359012 Click to see 326.40 unknown https://doi.org/10.1211/0022357001774949
https://doi.org/10.1007/BF02975429
https://doi.org/10.1248/BPB.26.1039
https://doi.org/10.1248/BPB.27.1147
https://doi.org/10.1016/S0031-9422(00)81847-6
Meso-Dihydroguaiaretic Acid 476856 Click to see 330.40 unknown https://doi.org/10.1248/BPB.28.2176
https://doi.org/10.1016/S0031-9422(00)81847-6
https://doi.org/10.1002/ARDP.19823151014
https://doi.org/10.1248/BPB.27.1147
https://doi.org/10.1271/BBB.62.1425
Meso-monomethyldihydroguaiaretic acid 11725068 Click to see 344.40 unknown https://doi.org/10.1248/BPB.27.1147
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1016/0031-9422(91)84145-I
5-[(3S,6S)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 25245913 Click to see 354.40 unknown via CMAUP database
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1007/BF02975429
Sesamin, (-)- 382073 Click to see 354.40 unknown https://doi.org/10.1211/0022357001774949
Syringaresinol 100067 Click to see 418.40 unknown https://doi.org/10.1021/NP2001896
https://doi.org/10.1016/0031-9422(91)84145-I
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Galbacin 11175182 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C 340.40 unknown https://doi.org/10.1007/BF02975429
https://doi.org/10.1248/BPB.27.1147
(+)-Galbacin 442873 Click to see 340.40 unknown https://doi.org/10.1211/0022357001774949
(2S,3S,4S,5S)-2,5-bis(3,4-dimethoxyphenyl)-3,4-dimethyloxolane 11975378 Click to see 372.50 unknown https://doi.org/10.1211/0022357001774949
https://doi.org/10.1007/BF02975429
2-(3-Methoxy-4-hydroxyphenyl)-5-(3,4-dimethoxyphenyl)-3,4-dimethyltetrahydrofuran 10066965 Click to see 358.40 unknown https://doi.org/10.1248/BPB.27.1147
https://doi.org/10.1016/0031-9422(88)83162-5
4-[(2S,3R,4S,5S)-5-(4-hydroxy-3-methoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 58507652 Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC)C 344.40 unknown https://doi.org/10.1016/0031-9422(88)83162-5
4-[(2S,3S,4R,5R)-5-(1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 13844301 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O)OC)C 342.40 unknown https://doi.org/10.1016/0031-9422(88)83162-5
4-[(2S,3S,4R,5R)-5-(3,4-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 13939326 Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)OC)OC)C 358.40 unknown https://doi.org/10.1007/BF02975429
https://doi.org/10.1211/0022357001774949
https://doi.org/10.1248/BPB.26.1039
https://doi.org/10.1248/BPB.27.1147
https://doi.org/10.1016/0031-9422(88)83162-5
4-[(3S,4R)-5-(3,4-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 5320040 Click to see 358.40 unknown https://doi.org/10.1016/S0031-9422(00)81847-6
4-[(3S,4R)-5-(4-hydroxy-3-methoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 5320041 Click to see 344.40 unknown https://doi.org/10.1007/BF02975429
https://doi.org/10.1211/0022357001774949
https://doi.org/10.1248/BPB.26.1039
https://doi.org/10.1016/S0031-9422(00)81847-6
4-[5-(1,3-Benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 13844298 Click to see 342.40 unknown https://doi.org/10.1016/0031-9422(88)83162-5
5-[5-(3,4-Dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-1,3-benzodioxole 12302263 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C 356.40 unknown https://doi.org/10.1016/0031-9422(88)83162-5
Fragransin C1 13870578 Click to see 374.40 unknown https://doi.org/10.1016/0031-9422(88)83162-5
Galbacin 234441 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C 340.40 unknown https://doi.org/10.1007/BF02975429
https://doi.org/10.1248/BPB.27.1147
Galbelgin 609882 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C 372.50 unknown via CMAUP database
Galgravin 101749 Click to see 372.50 unknown https://doi.org/10.1211/0022357001774949
https://doi.org/10.1007/BF02975429
Machilin G 10450921 Click to see 356.40 unknown https://doi.org/10.1211/0022357001774949
https://doi.org/10.1007/BF02975429
https://doi.org/10.1016/0031-9422(88)83162-5
Machilin I 13870573 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(88)83162-5
Malabaricano 13870570 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(88)83162-5
https://doi.org/10.1248/BPB.27.1147
Nectandrin B 156517 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(88)83162-5
https://doi.org/10.1211/0022357001774949
https://doi.org/10.1248/BPB.26.1039
https://doi.org/10.1007/BF02975429
https://doi.org/10.1248/BPB.27.1147
rel-(-)-(7S,7'R,8S,8'R)-4,4'-dihydroxy-3,3',5'-trimethoxy-7,7'-epoxylignan 53359707 Click to see 374.40 unknown https://doi.org/10.1016/0031-9422(88)83162-5
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5R)-2-[(2R,3R)-4-hydroxy-2,3-bis[(4-hydroxy-3,5-dimethoxyphenyl)methyl]butoxy]oxane-3,4,5-triol 14521030 Click to see 554.60 unknown https://doi.org/10.1016/0031-9422(91)84145-I
(2R,3R,4S,5R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 14521039 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O 552.60 unknown https://doi.org/10.1016/0031-9422(91)84145-I
Lyoniresinol, beta-D-xyloside; beta-D-Xylopyranoside, [1,2,3,4-tetrahydro-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-2-naphthalenyl]methyl, [1S-(1alpha,2beta,3alpha)]- 14521038 Click to see 552.60 unknown https://doi.org/10.1016/0031-9422(91)84145-I
Nudiposide 14521040 Click to see 552.60 unknown https://doi.org/10.1016/0031-9422(91)84145-I
Ssioriside 14521028 Click to see 554.60 unknown https://doi.org/10.1016/0031-9422(91)84145-I
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethylocta-1,3,7-triene 5320249 Click to see CC(=C)CCC=C(C)C=C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown via CMAUP database
cis-alpha-Ocimene 5463455 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4,11,11-Trimethyl-8-methylenebicyclo(7.2.0)undec-4-ene 26318 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-rel- 10583 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(3S,4aS,8aS)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene 12309813 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene 519361 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)88484-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Hecogenin 91453 Click to see 430.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16-diol 46865976 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18S)-15,16-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 10253011 Click to see 446.60 unknown via CMAUP database
Chlorogenin 12303065 Click to see 432.60 unknown via CMAUP database
Gitogenin 441887 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown via CMAUP database
Rockogenin 167555 Click to see 432.60 unknown via CMAUP database
Sarsasapogenin 92095 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown via CMAUP database
Smilagenin 91439 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown via CMAUP database
Tigogenin 99516 Click to see 416.60 unknown via CMAUP database
Yuccagenin 3083608 Click to see 430.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 6-hydroxysteroids
Methyl 3,6-dihydroxy-4-methoxy-2,2-dimethyl-3,4-dihydrobenzo[h]chromene-5-carboxylate 5319446 Click to see CC1(C(C(C2=C(O1)C3=CC=CC=C3C(=C2C(=O)OC)O)OC)O)C 332.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2R)-2-[(3S,7R,8S,9S,10R,13S,14S,16S,17R)-7-hydroxy-10,13-dimethyl-3,16-bis[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylheptan-4-one 101620741 Click to see 756.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18R)-16-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 101243911 Click to see 754.90 unknown via CMAUP database
(1R,2S,4S,6R,7S,8R,9S,12S,13S,16S,18R)-16-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 101784689 Click to see CC1C2C(CC3C2(C(=O)CC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)OC19CCC(=C)CO9 915.00 unknown via CMAUP database
(25R)-2beta-OH-timosaponin A III 10605143 Click to see 756.90 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2R)-4-[(1R,2S,4S,8S,9S,12S,13S,16S,18R)-16-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101784691 Click to see 903.10 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(3R,4R,5R,6S)-6-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18S)-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 71716476 Click to see 1197.30 unknown via CMAUP database
(2S,3R,4S,5R)-2-[(2S,3R,4S,5R,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxyoxane-3,4,5-triol 21625854 Click to see 1167.30 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-3-hydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21603422 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1 903.10 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13S,16S,18R)-10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 101784690 Click to see 756.90 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21603426 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1 740.90 unknown via CMAUP database
Smilagenin 3-O-beta-D-glucopyranosyl-(1->2)-[beta-D-glucopyranosyl-(1->3)]-beta-D-galactopyranoside 21603424 Click to see 903.10 unknown via CMAUP database
Smilagenin 3-O-beta-D-glucopyranosyl-(1->2)-beta-D-galactopyranoside 10628815 Click to see 740.90 unknown via CMAUP database
Timosaponin A-III 15953793 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1 740.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Norathyriol 5281656 Click to see 260.20 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(R)-Reticuline 440586 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown via CMAUP database
dl-N-Norarmepavine 317405 Click to see 299.40 unknown https://doi.org/10.1248/YAKUSHI1947.84.4_362
L-(-)-N-norarmepavine 6999736 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)OC 299.40 unknown https://doi.org/10.1248/YAKUSHI1947.84.4_362
> Organoheterocyclic compounds / Oxolanes
2-Octadecylidene-3-hydroxy-4-methylenebutanolide 11969969 Click to see CCCCCCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 364.60 unknown https://doi.org/10.1016/0031-9422(91)84145-I
4-Hydroxy-5-methylidene-3-octadecylideneoxolan-2-one 370916 Click to see CCCCCCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 364.60 unknown https://doi.org/10.1016/0031-9422(91)84145-I
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Acuminatin 6442251 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC(=C(C=C3)OC)OC 340.40 unknown https://doi.org/10.1211/0022357001774949
(-)-Licarin A 6442393 Click to see 326.40 unknown https://doi.org/10.1211/0022357001774949
https://doi.org/10.1016/S0031-9422(00)81847-6
https://doi.org/10.1007/BF02975429
https://doi.org/10.1016/0031-9422(91)84145-I
(-)-Licarin B 10860310 Click to see 324.40 unknown https://doi.org/10.1016/S0031-9422(00)81847-6
https://doi.org/10.1016/0031-9422(91)84145-I
(-)-Licarin-B 6441061 Click to see 324.40 unknown https://doi.org/10.1016/S0031-9422(00)81847-6
https://doi.org/10.1016/0031-9422(91)84145-I
(+)-Acuminatin 6441048 Click to see 340.40 unknown https://doi.org/10.1007/BF02975429
(+/-)-trans-Dehydrodiisoeugenol 73548 Click to see 326.40 unknown https://doi.org/10.1016/S0031-9422(00)81847-6
https://doi.org/10.1016/0031-9422(91)84145-I
(2'R,3R)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(E)-2-[(2'R,3R)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxospiro[1-benzofuran-3,3'-2H-1-benzofuran]-4-yl]ethenyl]spiro[1-benzofuran-3,3'-2H-1-benzofuran]-2-one 17757603 Click to see 810.70 unknown via CMAUP database
(2'R,3S)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(E)-2-[(2'R,3S)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxospiro[1-benzofuran-3,3'-2H-1-benzofuran]-4-yl]ethenyl]spiro[1-benzofuran-3,3'-2H-1-benzofuran]-2-one 17755939 Click to see 810.70 unknown via CMAUP database
(2R,3S)-2-(3,4-dimethoxyphenyl)-7-methoxy-3-methyl-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran 71763018 Click to see 340.40 unknown https://doi.org/10.1248/BPB.27.1147
(E)-3-[(2S,3S)-2-(1,3-benzodioxol-5-yl)-7-methoxy-3-methyl-2,3-dihydro-1-benzofuran-5-yl]prop-2-en-1-ol 13939331 Click to see CC1C(OC2=C1C=C(C=C2OC)C=CCO)C3=CC4=C(C=C3)OCO4 340.40 unknown https://doi.org/10.1016/S0031-9422(00)81847-6
2-(3,4-Dimethoxyphenyl)-7-methoxy-3-methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran 53934174 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC(=C(C=C3)OC)OC 340.40 unknown https://doi.org/10.1248/BPB.27.1147
2-(4-Hydroxy-3-methoxyphenyl)-7-methoxy-3-methyl-2,3-dihydro-1-benzofuran-5-carbaldehyde 15098590 Click to see CC1C(OC2=C1C=C(C=C2OC)C=O)C3=CC(=C(C=C3)O)OC 314.30 unknown https://doi.org/10.1248/BPB.27.1147
3-[2-(1,3-Benzodioxol-5-yl)-7-methoxy-3-methyl-2,3-dihydro-1-benzofuran-5-yl]prop-2-en-1-ol 162852866 Click to see 340.40 unknown https://doi.org/10.1016/S0031-9422(00)81847-6
5-(7-Methoxy-3-methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl)-1,3-benzodioxole 3398496 Click to see 324.40 unknown https://doi.org/10.1016/S0031-9422(00)81847-6
https://doi.org/10.1016/0031-9422(91)84145-I
5-[(3S)-7-methoxy-3-methyl-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]-1,3-benzodioxole 5384942 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC4=C(C=C3)OCO4 324.40 unknown https://doi.org/10.1016/S0031-9422(00)81847-6
https://doi.org/10.1016/0031-9422(91)84145-I
5-Benzofurancarboxaldehyde, 2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3-methyl-, trans- 101663167 Click to see 314.30 unknown https://doi.org/10.1248/BPB.27.1147
Gloriosaol D 102380006 Click to see COC1=C(C=C(C2=C1OC(=O)C23C(OC4=CC(=CC(=C34)O)O)C5=CC=C(C=C5)O)C=CC6=C7C(=CC(=C6)O)OC(=O)C78C(OC9=CC(=CC(=C89)O)O)C1=CC=C(C=C1)O)O 810.70 unknown via CMAUP database
Licarin A 5281836 Click to see 326.40 unknown https://doi.org/10.1211/0022357001774949
https://doi.org/10.1016/S0031-9422(00)81847-6
https://doi.org/10.1007/BF02975429
https://doi.org/10.1016/0031-9422(91)84145-I
> Phenylpropanoids and polyketides / Cinnamyl alcohols
[(1R,2R)-1-(1,3-benzodioxol-5-yl)-2-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenoxy]propyl] acetate 163190764 Click to see 400.40 unknown https://doi.org/10.1016/S0031-9422(00)81847-6
[1-(1,3-Benzodioxol-5-yl)-2-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]propyl] acetate 163013069 Click to see CC(C(C1=CC2=C(C=C1)OCO2)OC(=O)C)OC3=C(C=C(C=C3)C=CCO)OC 400.40 unknown https://doi.org/10.1016/S0031-9422(00)81847-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(91)84145-I
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1016/0031-9422(91)84145-I
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/0031-9422(91)84145-I
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1016/0031-9422(91)84145-I
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1016/0031-9422(91)84145-I
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1016/0031-9422(91)84145-I
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2S,3R,4S,5S,6R)-2-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-chroman-5-yl]oxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol 10343835 Click to see C1C(C(OC2=C1C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 44259215 Click to see 434.30 unknown https://doi.org/10.1177/1934578X1501000817
Afzelin 5316673 Click to see 432.40 unknown https://doi.org/10.1177/1934578X1501000817
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1177/1934578X1501000817
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-3-methyl-3,4-dihydro-2H-chromene-5,7-diol 44445800 Click to see 288.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4Z,6R,7R)-4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6-methyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 12311394 Click to see 351.40 unknown via CMAUP database

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